| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:5612024-5612637 | Common:5; Rare:253 | ||||
| chr12:6020910-6021260 | Common:6; Rare:67 | ||||
| chr12:6065188-6065666 | Common:6; Rare:267; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:6070910-6071310 | Common:1; Rare:86 | ||||
| chr12:6084680-6085020 | Common:3; Rare:62 | ||||
| chr12:6089070-6089460 | Common:5; Rare:138 | ||||
| chr12:6182030-6182750 | Common:11; Rare:252 | ||||
| chr12:6201529-6202275 | Common:5; Rare:204 | ||||
| chr12:6215980-6216238 | Rare:63 | ||||
| chr12:6221291-6222697 | Common:25; Rare:482 | ||||
| chr12:6228986-6229207 | Rare:31 | ||||
| chr12:6229400-6229780 | Common:7; Rare:129 | ||||
| chr12:6235101-6235591 | Common:4; Rare:238 | ||||
| chr12:6235675-6235897 | Rare:42 | ||||
| chr12:6237503-6237943 | Common:8; Rare:336 |